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2000
Volume 9, Issue 2
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Oligonucleotide analogs with L- and D-lysine residues incorporated in internucleotide linkages were synthesized and their affinity toward complementary DNA was studied. Stability of the duplexes formed by the modified oligonucleotides and their wild-type complements appeared to be close to that of the isosequential unmodified duplex, oligonucleotides carrying D-lysine residues forming generally more stable duplexes than L-lysine derivatives.

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/content/journals/loc/10.2174/157017812800221799
2012-02-01
2025-10-15
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